行为和神经内分泌可塑性的赢家和输家的影响形式

Nathaniel S. Rieger, Matthew J. Fuxjager, B. Trainor, Xin Zhao, C. Marler
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引用次数: 2

摘要

动物的社会生活是复杂的。生活在大群体中的个体不仅必须驾驭各种从属关系,还必须驾驭各种敌对关系(Oliveira, 2009)。此外,一个人的社会景观总是在不断变化,随着一年中的时间、人口密度和其他随机环境扰动而变化。因此,支持社会敏捷性和灵活性的行为和生理/神经机制应该进化,以允许个人调整他们的行为。研究这一框架的一种方法是研究行为和生理可塑性的两种相关现象:赢家效应和输家效应。赢家效应被定义为在获得先前的社会胜利后赢得战斗的能力,而失败者效应被定义为在先前的社会失败后失败的倾向增加。这两个行为过程本质上都是心理上的,因此每个过程都可能独立于内在的战斗能力而发生(Hsu & Wolf, 1999)。事实上,Hsu, Early和Wolf(2006)在一篇重要的赢家和输家效应综合文献中指出,个体形成赢家效应是因为他们更愿意参与战斗,而不是通过改变内在能力来变得更快或更强。同样的情况也发生在失败者效应中:个体变得更有可能失败,因为他们认为自己是失败者,而不是因为某种原因而变得更慢或更弱。赢家和输家效应存在于各种各样的分类群中,包括哺乳动物(Huhman et al., 2003;Oyegbile and Marler, 2005),爬行动物(Schuett, 1997),鸟类(Apfelbeck, Stegherr, & Goymann, 2011;Drummond & Canales, 1998;Popp, 1988), fish (Bakker, Feuthdebruijn, & Sevenster, 1989;Bakker & Sevenster, 1983;比彻姆,1988;Beaugrand, Goulet, & Payette, 1991;Chase, Tovey, Spangler-Martin, & Manfredonia, 2002)和无脊椎动物(Bergman et al., 2003;Hoefl, 2002;怀特豪斯出版社,1997)。一些研究甚至表明,人类形成了赢家和输家效应(Yee, Bailenson, & Duchenaut, 2009),而其他研究则考虑了这些效应如何波及并对社会行为产生更广泛的影响(Coates, Gurnell, & Sarnyai, 2010)。此外,对这两种现象的荟萃分析指出,它们不一定同时发生——某些物种可能会表现出输家效应,但不会表现出赢家效应(Hsu et al., 2006;
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Behavioral and neuroendocrine plasticity in the form of winner and loser effects
The social lives of animals are complex. Individuals living in large populations must not only navigate a variety of affi liative relationships but also a wide range of adversarial ones ( Oliveira, 2009 ). Furthermore, one’s social landscape is always in fl ux, changing in response to time of year, population density, and other stochastic environmental perturbations. Accordingly, behavioral and physiological/neural mechanisms that support social agility and fl exibility should evolve to allow individuals to fi ne-tune their behavior. One way that research has focused on this framework is by studying two related phenomena that epitomize behavioral and physiological plasticity: the winner effect and the loser effect. The winner effect is defi ned as an ability to win fi ghts following the acquisition of prior social victories, whereas the loser effect is defi ned as an increased propensity to lose fi ghts following prior social defeat. Both behavioral processes are psychological in nature, and thus each potentially can occur independently of intrinsic fi ghting ability (Hsu & Wolf, 1999). Indeed, in an important synthesis of the winner and loser effect literature, Hsu, Early and Wolf (2006 ) point out that individuals form a winner effect because they have a greater willingness to engage in a fi ght rather than by necessarily changing intrinsic ability to become faster or stronger. The same is thought to occur for the loser effect: individuals become more likely to lose because they perceive themselves as losers, as opposed to somehow becoming intrinsically slower or weaker. Winner and loser effects are found in a wide variety of taxa, including mammals ( Huhman et al., 2003 ; Oyegbile and Marler, 2005 ), reptiles ( Schuett, 1997 ), birds ( Apfelbeck, Stegherr, & Goymann, 2011 ; Drummond & Canales, 1998 ; Popp, 1988 ), fi sh ( Bakker, Feuthdebruijn, & Sevenster, 1989 ; Bakker & Sevenster, 1983 ; Beacham, 1988 ; Beaugrand, Goulet, & Payette, 1991 ; Chase, Tovey, Spangler-Martin, & Manfredonia, 2002 ), and invertebrates ( Bergman et al., 2003 ; Hoefl er, 2002 ; Whitehouse, 1997 ). Some work even suggests that humans form winner and loser effects ( Yee, Bailenson, & Duchenaut, 2009 ), while other studies have considered how these effects can ripple out and have broader effects on social behavior ( Coates, Gurnell, & Sarnyai, 2010 ). Additionally, meta-analyses of these two phenomena point out that they need not occur together – some species might show a loser effect, but not a winner effect ( Hsu et al., 2006 ;
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